Polyester film containing minute glass spheres and fumed silica

ABSTRACT

The present invention relates to films or sheets of linear polyester containing glass spheres having a certain particle size distribution and in a certain amount based upon the weight of the polyester film. The addition of the glass spheres improves several properties of the film, including the dynamic coefficient of friction. Preferably, a second film additive, fumed silica, of a controlled particle size distribution and weight is additionally added to the film. The addition of the fumed silica additionally improves several properties of the polyester film, including the static coefficient of friction of the film.

This application is a of Ser. No. 07/613,183 filed Nov. 14, 1990, nowabandoned.

BACKGROUND OF THE INVENTION

Films or sheets of linear polyester have been commercially available formany years. The film has excellent draw orientation and has proved to beespecially well suited for the biaxial film orientation processresulting in films of outstanding properties. The film is also known aspolyethylene terephthalate or PET and is strong and has excellentinherent chemical and thermal stability properties. The polymerpreparation and film manufacturing processes are well known to thoseskilled in the art and are recited in many texts, including theEncyclopedia of Polymer Science and Engineering, second edition, volume12, by John Wiley and Sons, Inc., pages 1 through 313; and numerous U.S.and foreign patents.

The myriad uses of polyester film have resulted in the need formodification of the basic film to provide special properties such asimproved slip and improved release properties. The control of surfaceslip is one of the prime requirements for the commercial use ofpolyester film. Slip is critical to the processability of the film,especially thin film. In the past, slip has been controlled byincorporating organic and inorganic filters to enhance surfaceroughness. However, the addition of these additives has caused increasedhaze in the film. These additives include inert particles such assilicas, china clay, aluminum silicates, calcium phosphates and glassparticles. The addition of these fillers improves the winding andslitting properties of the polyester film, however, their presence inthe film produces large surface asperities which makes polyester filmunsuitable for demanding applications such as when the film ismetallized with aluminum or gold and an absolutely smooth metallizedsurface is required. Examples of metallized films requiring a smoothsurface are polyester films used for solar window applications orcertain films demanding certain aesthetic properties.

U.S. Pat. No. 4,274,025 teaches a linear polyester film containingparticles of inorganic material that has an improved resistance tofibrillation, delamination, and tearing. Included is a listing of theinorganic materials synthetic silica, calcium borate, calcium carbonate,magnesium carbonate, barium sulphate, calcium or aluminum silicate andglass beads. The particle size for the inorganic material is between 2to 10 microns, but the amount of additive is stated to range between2000 to 9000 parts per million (ppm) based upon the weight of the film.The patent teaches that adding less than 2000 ppm does not render thefilm surface sufficiently rough to promote a satisfactory sliding actionfor good slip or frictional purposes. Quite surprisingly, the linearpolyester film of the present invention has excellent slip propertiesand it contains glass spheres in an amount 1000 times less than taughtfor U.S. Pat. No. 4,274,025.

U.S. Pat. No. 4,375,494 teaches a polyester film composite of a highlycrystalline, molecularly oriented first layer of linear polyester, aheat sealable second layer, adherent to the first layer, of an amorphouslinear polyester. The second layer contains from 50 to 2000 ppm (basedupon the weight of the second layer) of a finely-divided particulateadditive having an average particle size in the range of 2 to 10 micronstogether with 1000 to 10,000 ppm (based upon the weight of the secondfilm) of smaller, finely divided particles having an average particle inthe range of 0.005 to 1.8 microns. Both particulate additives aresubstantially uniformly dispersed throughout the second layer. Theparticulate additive is stated to be natural or synthetic silica, glassbeads, calcium borate, calcium carbonate, magnesium carbonate, bariumsulphate, calcium silicate, calcium phosphate, aluminum trihydride,aluminum silicates and titanium oxide or certain polymeric materials.Ideally, the particles are substantially spherical in shape. Theaddition of the additives to the second layer results in a film havingimproved handling, heat sealing properties, and anti-blockingproperties.

The amount of additives used in the film composite of this patent aremuch greater than the amount of additive material that has been found tobe useful in the practice of the present invention.

SUMMARY OF THE INVENTION

The present invention relates to films or sheets of linear polyestercontaining glass spheres having a certain particle size distribution andin a certain amount based upon the weight of the polyester film. Theaddition of the glass spheres improves several properties of the film,including the dynamic coefficient of friction.

Preferably, a second additive, fumed silica, of a controlled particlesize distribution and weight is additionally added to the film. Theaddition of the fumed silica additionally improves several properties ofthe polyester film, including the static coefficient of friction of thefilm.

DETAILED DESCRIPTION OF THE INVENTION

One embodiment of the present invention relates to a film of a linearpolyester containing minute glass spheres having an average particlesize of about 2 to about 3 microns (D₅₀ =2-3 microns) and a particledistribution as follows: 99.9% below about 8 microns (μm), 75% belowabout 5 microns, and 50% below about 2 microns. The glass spheres arepresent in an extremely small amount that ranges between about 1 partper million (ppm) to about 30 parts per million based upon the weight ofthe film; preferably the amount of glass spheres ranges between about 3ppm to about 30 ppm and more preferably the amount ranges between about6 ppm to about 20 ppm per weight of the film.

A film of linear polyester containing glass spheres of the abovedescribed particle distribution and weight will have improved handlingproperties, such as improved winding and slitting properties. As animprovement over prior art films of polyester having incorporatedtherein particles having similar particle size glass spheres but beingpresent in very large amounts ranging from 0.2 to 0.9 percent by weightbased upon the weight of the film, the film of the present inventiondoes not have large surface asperities which render the film undesirablein certain applications such as where a smooth metallized film compositeis required. For example, the film of polyester of the present inventionwhen subsequently metallized film will be free of defects such aswinding faults, blocking pimples, arrowheads or needles on the filmsurface.

Another embodiment of the present invention relates to a film ofpolyester containing the above described glass spheres in the particlesize distribution and weight as described in the first embodiment and,in addition, containing as a second film additive agglomerated fumedsilica particles having a particle size distribution of 100% below onemicron with the average particle size range being between about 0.10 toabout 0.50 microns and in an amount that ranges between about 0.01 toabout 0.02 percent (%) by weight based upon the weight of the film.Preferably, the particle size distribution of the agglomerated fumedsilica particles is 100% below one micron with the average particle sizeranging between about 0.20 to about 0.40 microns. Preferably, the amountof fumed silica that is present in the film ranges between about 0.015to about 0.018% by weight based upon the weight of the film. Preferably,the particle size distribution of the aggolmerated fumed silicaparticles is 100% below one micron with the average particle sizeranging between about 0.25 to about 0.35 microns. The individual ordiscrete fumed silica particles that go into the above describedagglomerates of fumed silica particles generally have a particle size ofaround 0.05 microns. However, as discussed previously, fumed silicararely exists as such small, discrete particles. Such small sizedparticles usually exist as agglomerates of 2 or more discrete particles.

Film of polyester having both the glass sphere and fumed silicaadditives will have a refractive index that is very close to therefractive index of biaxially oriented polyester film containing noadditives. Such film is very, very clear and thus it has a minimumamount of haze. Also, the addition of the fumed silica in the particlesize distribution and amount described above results in a film having animproved static coefficient of friction.

The glass spheres that are useful in the practice of the invention arecommercially sold and have a particle size distribution as measured byconventional apparatus such as a Malvern particle size analyzer. Theglass spheres are a solid glass sphere and are not limited to anychemical composition and they can have either a smooth surface or anetched surface. The surface can be etched by contacting the glassspheres with nitric acid for a time sufficient to give the desireddegree of etching of the surface. The glass spheres having the etchedsurface are preferred. The glass spheres are substantially spherical inshape with the particle size in microns referring to the diameter of theglass spheres. Preferred glass spheres are sold under the trade nameSpheriglass® and are sold by Potters Industries Inc., an affiliate ofthe PQ Corporation.

Fumed silica is formed when silicone tetrachloride reacts in a hydrogenflame to form single, spherical droplets of silicone dioxide. These growthrough collision and coalescence to form layer droplets. As thedroplets cool and begin to freeze, but continue to collide, they stickbut do not coalesce, forming solid aggregates which in turn continue tocollide to form clusters which are known as agglomerates. The particlesize for the fumed silica refers to the particle size of a single cooledspherical droplet.

The required quantities of glass spheres and fumed silica can be addedto the film of polyester forming material at any point in the filmmanufacturing process prior to the extrusion of the polymer. In thegeneral practice of this invention, it is preferred to incorporate theglass spheres and fumed silica particles into the polyester during itsproduction by polymerization. A convenient procedure is to add theparticles to the polycondensation mixture used for the production of thepolyester. It has been found particularly desirable to add the glassspheres and fumed silica during the manufacture of the polyester polymeras a slurry after the ester interchange reaction in which monomers areformed. The particles can, for example, be added as a slurry in theglycol from which the polyester is formed prior to the commencement ofthe polycondensation.

The polymer useful in the manufacture of a film of a synthetic linearpolyester is well known to those skilled in the art and may be obtainedby condensing one or more dicarboxylic acids or their lower alkyl (up to6 carbon atoms) diesters, eg. terephthalic acid, isophthalic acid,phthalic acid, 2,5-, 2,6- or 2,7-naphthalenedicarboxylic acid, succinicacid, sebacic acid, adipic acid, azelaic acid, 4,4'-diphenyldicarboxylicacid, hexahydroterephthalic acid or 1,2-bis-p-carboxyphenoxyethane(optionally with a monocarboxylic acid, such as pivalic acid) with oneor more glycols, eg. ethylene glycol, 1,3-propanediol, 1,4-butanediol,neopentyl glycol and 1,4-cyclohexanedimethanol.

The polyester film prepared from the composition according to thepresent invention may be uniaxially or biaxially oriented, but ispreferably biaxially oriented by drawing in two mutually perpendiculardirections in the plane of the film to achieve a satisfactorycombination of mechanical and physical properties. Preferably, the filmis biaxially oriented by sequential stretching in two mutuallyperpendicular directions, typically at a temperature in the range of 70°to 250° C. Such stretching is described in many patents, includingBritish Patent No. 838,708. These techniques are well known to thoseskilled in the polyester film manufacture art.

A conventional coating medium may optionally be applied to the polyesterfilm. Such coatings are customarily added to improve the adhesive oranti-static properties. The chemical compositions of these coatings arewell known to those skilled in the art and are described in numerouspatents and publications. The coating medium may be applied to anuniaxially oriented or a biaxially oriented film substrate. In asimultaneous biaxially oriented stretching process, the coating mediumis suitably applied to the substrate either before commencement or afterconclusion of the stretching operation. In a sequential biaxiallyoriented stretching process, preferably the coating medium is applied tothe film substrate between the two stretching stages i.e. between thelongitudinal and transverse stretchings of a biaxial stretchingoperation. Such a sequence of stretching and coating is especiallypreferred for the production of a coated polyethylene terephthalatefilm. Preferably the film is first stretched in the longitudinaldirection over a series of rotating rollers, then coated with thecoating medium, and lastly stretched transversely in a stenter oven,preferably followed by heat setting of the coated film.

The optional coating medium may be applied to the polyester film as anaqueous dispersion or solution in an organic solvent by any suitableconventional coating technique such as by dip coating, bead coating,reverse roller coating or slot coating.

The temperatures applied to the coated film during the subsequentstretching and/or heat setting are effective in drying the aqueousmedium, or the solvent in the case of solvent-applied compositions, andalso in coalescing and forming the coating into a continuous and uniformlayer.

A preferred adhesion coating or layer for the polyester film accordingto the invention is manufactured from film-forming adhesion layerpolymers providing superior adhesion properties. Suitable adhesion layerpolymers comprise at least one monomer derived from an ester of acrylicacid, especially an alkyl ester where the alkyl group contains up to tencarbon atoms such as methyl, ethyl, n-propyl, isopropyl, n-butyl,isobutyl, terbutyl, hexyl, 2-ethylhexyl, heptyl, and n-octyl. Polymersderived from an alkyl acrylate, for example ethyl acrylate and butylacrylate, together with an alkyl methacrylate are preferred. Polymerscomprising ethyl acrylate and methyl methacrylate are particularlypreferred. The acrylate monomer is preferably present in a proportion inthe range of 30 to 65 mole %, and the methacrylate monomer is preferablypresent in a proportion in the range of 20 to 60 mole %.

Other monomers which are suitable for use in the preparation of theadhesion layer polymer, which may be preferably copolymerized asoptional additional monomers together with esters of acrylic acid and/ormethacrylic acid, and derivatives thereof, include acrylonitrile,methacrylonitrile, halo-substituted acrylonitrile, halo-substitutedmethacrylonitrile, acrylamide, methacrylamide, N-methylol acrylamide,N-ethanol acrylamide, N-propanol acrylamide, N-methacrylamide, N-ethanolmethacrylamide, N-methyl acrylamide, N-tertiary butyl acrylamide,hydroxyethyl methacrylate, glycidyl acrylate, glycidyl methacrylate,dimethylamino ethyl methacrylate, itaconic acid, itaconic anhydride andhalf esters of itaconic acid.

Other optional monomers of the adhesion layer polymer include vinylesters such as vinyl acetate, vinyl chloracetate and vinyl benzoate,vinyl pyridine, vinyl chloride, vinylidene chloride, maleic acid, maleicanhydride, styrene and derivatives of styrene such as chloro styrene,hydroxy styrene and alkylated styrenes, wherein the alkyl group containsfrom one to ten carbon atoms.

A preferred adhesion layer polymer is derived from 3 monomers: (1) 35 to60 mole % ethyl acrylate, (2) 30 to 55 mole % methyl methacrylate, and(3) 2 to 20 mole % methacrylamide.

The molecular weight of the adhesion layer polymer can vary over a widerange, but is preferably within the range 40,000 to 300,000, and morepreferably within the range 50,000 to 200,000.

If desired, the optional coating composition may also contain across-linking agent which functions to form cross-links within thecoating layer thereby improving adhesion to the polymeric filmsubstrate. Additionally, the cross-linking agent should preferably becapable of internal cross-linking in order to provide protection againstsolvent penetration. The cross-linking of cross-linkable coatingcompositions can be achieved at the conventional stretching and/orheat-setting temperatures. Suitable cross-linking agents may compriseepoxy resins, alkyd resins, amine derivatives such as hexamethoxymethylmelamine, and/or condensation products of an amine, eg. melamine,diazine, urea, cyclic ethylene urea, cyclic propylene urea, thiourea,cyclic ethylene thiourea, alkyl melamines, aryl melamines, benzoguanamines, guanamines, alkyl guanamines and aryl guanamines, with analdehyde, eg. formaldehyde. A useful condensation product is that ofmelamine with formaldehyde.

The condensation product may optionally be alkoxylated. Thecross-linking agent may be used in amounts of up to 25% by weight basedon the weight of the polymer in the optional coating composition. Acatalyst is also preferably employed to facilitate cross-linking actionof the cross-linking agent. Preferred catalysts for cross-linkingmelamine formaldehyde include ammonium chloride, ammonium nitrate,ammonium thiocyanate, ammonium dihydrogen phosphate, ammonium sulphate,diammonium hydrogen phosphate, para toluene sulphonic acid, maleic acidstabilized by reaction with a base, and morpholinium para toluenesulphonate.

Preferably, the uncoated polyester film of this invention ismanufactured so that it has a thickness of about 98 to 500 gauge.

The coating layer is preferably applied to the polyester film at a coatweight within the range 0.1 to 10 mgdm⁻², especially 0.5 to 2.0 mgdm⁻².

The ratio of the thickness of the polyester substrate to the thicknessof the coating layer can vary within a wide range, although thethickness of the coating layer preferably should not be less than 0.004%nor greater than 10% of that of the substrate. In practice, thethickness of the coating layer is desirably at least 0.01 micron andpreferably should not exceed about 1.0 micron.

Prior to deposition of the coating layer onto the polyester substrate,the exposed surface thereof may, if desired, be subjected to a chemicalor physical surface-modifying treatment to improve the bond between thatsurface and the subsequently applied coating layer. Modification of thesubstrate surface may for example be by flame treatment, ionbombardment, electron beam treatment or ultra-violet light treatment. Apreferred treatment, because of its simplicity and effectiveness is tosubject the exposed surface of the substrate to a high voltageelectrical stress accompanied by corona discharge. Alternatively, thesubstrate may be pretreated with an agent known in the art to have asolvent or swelling action on the substrate polymer. Examples of suchagents, which are particularly suitable for the treatment of a polyestersubstrate, include a halogenated phenol dissolved in a common organicsolvent eg. a solution of p-chloro-m-cresol, 2,4-dichlorophenol, 2,4,5-or 2,4,6-trichlorophenol or 4-chlororesorcinol in acetone or methanol.

The optional coating layer may be applied to one or both surfaces of thepolyester substrate, and one or both coating layers may be subjected tocoating with additional material. The function of the original coatinglayer may thus be as a primer layer to aid the subsequent deposition ofadditional coating layer(s).

The one or more polymeric layers of the polyester film substrate and anyoptional coating layers used to form a composition may convenientlycontain any of the additives conventionally employed in the manufactureof thermoplastics polyester films. Thus, such agents as dyes, pigments,voiding agents, lubricants, anti-oxidants, anti-blocking agents, surfaceactive agents, slip aids, gloss-improvers, prodegradants, ultra-violetlight stabilizers, viscosity modifiers and dispersion stabilizers may beincorporated in the polyester film substrate and/or coating layer(s), asappropriate.

The invention can be better understood by referring to the followingspecific examples which teach the several embodiments of this invention.

EXAMPLE 1

Commercially solid glass spheres, sold by Potters Industries Inc. asSPHERIGLASS® E250P2BH having a particle size distribution of 99.9percent below 7.2 microns, 75 percent below 5 microns and 50 percentbelow 2.0 microns and an average particle size of 2.2 microns (D₅₀ =2.2microns) were mixed with ethylene glycol to form a slurry having a 1.0%solid. The slurry was mixed under high shear in a 5 gallon Ross Mixerfor one hour. The mixed slurry was pumped into the bishydroxyethyleneterephthalate (monomer) that is used in the commercial preparation ofpolyethylene terephthalate. The glass spheres were added in quantitiessuch that 6 ppm were found in the resulting extruded film. After theaddition of glass spheres, conventional polymerization catalysts wereadded to the reaction mixture. The resulting PET polymer was extrudedonto a cooled quenched surface and biaxially oriented by conventionalfilm manufacturing techniques. The molten monomer was then polymerizedat 285°-290° C. at a pressure of about 0.5 millimeters of mercury. Theresulting polyethylene terephthalate was cooled and converted to chips.

The dried chips were then extruded at 285° C. into film and thenbiaxially oriented by stretching in sequence in mutually perpendiculardirections at draw directions of about 2.9:1 in each direction followedby heat setting at 225° C. The resulting filled film product had a totalthickness of 200 gauge and was evaluated for optical properties ascompared to an identical unfilled 200 gauge film made of the samepolyester polymer and manufactured by the same procedure. Both films hadan extremely low bulk haze of 0.25% as measured by the GardnerHazemeter. In addition to excellent clarity, the filled polyester filmhad excellent gloss. The filled film was also evaluated for windingcharacteristics and found to produce smooth mill rolls at high windingspeeds with no observable interfacial sticking surface blemishes such asarrowheads, blocking pimples, needles, or telescoping. The filled filmwas metallized with aluminum using conventional techniques and thealuminum surface was found to have no speckles.

EXAMPLE 2

A second filled biaxially oriented polyethylene terephthalate(polyester) film was prepared by the procedures of Example 1 but variedby incorporating 6 ppm of the glass spheres used in Example 1 and 165ppm fumed silica, Aerosil® OX50 sold by the DeGussa Company. The fumedsilica had a discrete particle size of 0.050 microns. Ethylene glycolslurries of the fumed silica and the glass spheres were prepared in aRoss high speed mixer at concentrations of 4% and 1% solids,respectively. The slurries were added to the molten monomer. The moltenmonomer was then polymerized at 285°-290° C. at a pressure of about 0.5millimeters of mercury. The resulting polyethylene terephthalate wascooled and converted to chips.

The dried chips were then extruded at 285° C. into film and thenbiaxially oriented by stretching in sequence in mutually perpendiculardirections at draw directions of about 2.9:1 in each direction followedby heat setting at 225° C. having a thickness of 200 gauge. The film wasevaluated for winding and optical characteristics and was found toexhibit excellent optical and winding performance. Compared to theunfilled film prepared in Example 1, there was a slight depreciation infilm clarity (0.3% for 200 gauge film versus 0.25% in Example 1) butstill the clarity was excellent.

EXAMPLE 3

Another filled biaxially oriented polyethylene terephthalate (polyester)film was prepared by incorporating 3 ppm of the glass spheres used inExample 1 and 83 ppm of the fumed silica used in Example 2. Ethyleneglycol slurries of the fumed silica and the glass sphere were preparedin a Ross high speed mixer at concentrations of 4% and 1% solids,respectively. The slurries were added to the molten monomer. The moltenmonomer was then polymerized at 285°-290° C. at a pressure of about 0.5millimeters of mercury. The resulting polyethylene terephthalate wascooled and converted to chips.

The dried chips were then extruded at 285° C. into film and thenbiaxially oriented by stretching in sequence in mutually perpendiculardirections at draw directions of about 2.9:1 in each direction followedby heat setting at 225° C. having a thickness of 200 gauge. The film wasevaluated for winding and optical characteristics and was found toexhibit excellent optical and winding performance. Compared to theunfilled film prepared in Example 1, the clarity was almost identicaland good winding characteristics were obtained.

EXAMPLE 4

Example 3 was repeated except that 6 ppm of commercially solid glassspheres, sold by Potters Industries Inc. as SPHERIGLASS® E250P2BH and165 ppm of Cab-o-sil L90 (primary particle size 27nm, and averageagglomerate size=220 to 250 nm) sold by Cabot Corporation were used asthe filler. Again, film was obtained that had excellent optical clarityand good winding characteristics. No "speckle" was observed aftermetallizing the film with aluminum and also with gold.

EXAMPLE 5

Films produced in Examples 1 through 3 were coated on one side with aconventional antistatic coating composition. Films were obtained withexcellent clarity, good winding and antistatic properties. No "speckle"was observed after metallizing the uncoated side of the film withaluminum and also with gold.

EXAMPLE 6

Films produced in Examples 1 through 3 were coated on one side with aconventional adhesion promoting coating. Films were obtained that hadgood clarity, good winding and good adhesion properties. No "speckle"was observed after metallizing the film on the uncoated side withaluminum and also with gold.

I claim:
 1. A film of linear oriented and heat set polyester containing(a) glass spheres having an average particle size of about 2 to about 3microns and a particle size distribution of 99.9 percent below about 8microns, 75 percent below about 5 microns and 50 percent below about 2microns, in an amount that ranges between about 1 part per million toabout 30 parts per million based upon the weight of the film of linearpolyester and (b) fumed silica having a discrete particle sizedistribution of 100 percent below 1 micron with the average discreteparticle size ranging between about 0.10 to about 0.50 microns in anamount that ranges between about 0.01 to about 0.02 percent by weightbased upon the weight of the film of linear polyester.
 2. The film oflinear polyester of claim 1 wherein the weight range of the glassspheres is between about 3 parts per million and about 30 parts permillion and the discrete particle size distribution of the fumed silicais 100 percent below 1 micron with the average discrete particle sizebeing in the range between about 0.20 microns to about 0.40 microns. 3.The film of linear polyester of claim 1 wherein the weight range of theglass spheres is between about 6 parts per million and about 20 partsper million and the discrete particle size range distribution of thefumed silica is 100 percent below 1 micron with the average discreteparticle size being in a range between about 0.25 to about 0.35 microns.4. The film of claim 3 wherein the amount of fumed silica that ispresent in the film ranges between about 0.15 to about 0.18 percent byweight based upon the weight of the film.
 5. The film of claim 3 whereinthe glass spheres are etched and the film is of a thickness of about 48to about 500 gauge.